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2-Methyl-4-(o-nitrobenzylidene)oxazol-5-ones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The cis and trans isomers of 2-methyl-4-(o-nitrobenzylidene)oxazol-5-one have been obtained. On reduction, the cis isomer formed 3-acetamidoquinolin-2-ol, and the trans isomer formed 4-(o-aminobenzylidene)-2-methyloxazol-5-one. Details of the IR, UV, PMR, and mass spectra of the compounds obtained are given.

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Literature cited

  1. S. N. Lur'e, E. S. Chumak, and T. A. Ravdel', Zh. Obshch. Khim., 23, 1392 (1953).

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Authors and Affiliations

  1. Physicochemical Institute, Academy of Sciences of the Ukrainian SSR, Odessa

    A. A. Mazurov, S. A. Andronati & V. V. Antonenko

Authors
  1. A. A. Mazurov
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  2. S. A. Andronati
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  3. V. V. Antonenko
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 615–617 (1985).

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Mazurov, A.A., Andronati, S.A. & Antonenko, V.V. 2-Methyl-4-(o-nitrobenzylidene)oxazol-5-ones. Chem Heterocycl Compd 21, 514–515 (1985). https://doi.org/10.1007/BF00506062

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  • DOI: https://doi.org/10.1007/BF00506062

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